Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10012
rs10012
8 0.769 0.214 2 38075247 missense variant G/C snp 0.31 0.36 0.010 1.000 1 2008 2008
dbSNP: rs1024611
rs1024611
14 0.734 0.429 17 34252769 intergenic variant A/G snp 0.28 0.010 1.000 1 2015 2015
dbSNP: rs1034528
rs1034528
4 0.846 0.107 1 11189075 intron variant G/C snp 0.30 0.010 1.000 1 2014 2014
dbSNP: rs1042522
rs1042522
56 0.563 0.643 17 7676154 stop gained G/C,T snp 0.67 0.62 0.010 1.000 1 2010 2010
dbSNP: rs1042636
rs1042636
15 0.715 0.286 3 122284922 missense variant A/G snp 0.15 0.10 0.010 1.000 1 2011 2011
dbSNP: rs10426628
rs10426628
2 0.923 0.071 19 48589173 intron variant A/G snp 0.77 0.010 1.000 1 2015 2015
dbSNP: rs10432782
rs10432782
6 0.821 0.107 21 31664078 intron variant T/G snp 0.19 0.010 1.000 1 2011 2011
dbSNP: rs1045485
rs1045485
26 0.652 0.393 2 201284866 missense variant G/A,C,T snp 4.0E-06; 9.0E-02 3.2E-05; 9.8E-02 0.010 1.000 1 2010 2010
dbSNP: rs1045531
rs1045531
2 0.923 0.071 8 142682129 synonymous variant C/A snp 0.45 0.44 0.010 1.000 1 2011 2011
dbSNP: rs10459592
rs10459592
2 0.923 0.071 15 51243944 intron variant T/G snp 0.50 0.010 1.000 1 2014 2014
dbSNP: rs1047303
rs1047303
3 0.878 0.107 1 119514623 missense variant C/A snp 0.75 0.77 0.010 1.000 1 2002 2002
dbSNP: rs1047768
rs1047768
5 0.821 0.143 13 102852167 synonymous variant T/C snp 0.52 0.59 0.010 1.000 1 2018 2018
dbSNP: rs10505346
rs10505346
2 0.923 0.071 8 118951604 intron variant G/T snp 0.21 0.010 1.000 1 2010 2010
dbSNP: rs1058587
rs1058587
4 0.878 0.179 19 18388612 missense variant C/G,T snp 0.24; 9.1E-06 0.23 0.010 1.000 1 2006 2006
dbSNP: rs1060501201
rs1060501201
3 0.923 0.071 17 7674190 missense variant T/C snp 0.010 1.000 1 2017 2017
dbSNP: rs10740051
rs10740051
2 0.923 0.071 10 46025670 intron variant C/T snp 0.24 0.010 1.000 1 2011 2011
dbSNP: rs10759932
rs10759932
7 0.784 0.179 9 117702866 intergenic variant T/C snp 0.19 0.010 1.000 1 2007 2007
dbSNP: rs10761581
rs10761581
2 0.923 0.071 10 46027444 missense variant A/C snp 0.44 0.41 0.010 1.000 1 2011 2011
dbSNP: rs10895304
rs10895304
2 0.923 0.071 11 102519261 intergenic variant A/G snp 0.19 0.010 1.000 1 2011 2011
dbSNP: rs10899221
rs10899221
2 0.923 0.071 11 76470587 intron variant G/A snp 6.3E-02 0.010 1.000 1 2014 2014
dbSNP: rs10948059
rs10948059
2 0.923 0.071 6 42960723 regulatory region variant C/G,T snp 0.39 0.46 0.010 1.000 1 2015 2015
dbSNP: rs10987883
rs10987883
2 0.923 0.071 9 128118550 non coding transcript exon variant G/A snp 0.83 0.010 1.000 1 2011 2011
dbSNP: rs11063118
rs11063118
2 0.923 0.071 12 4372398 intron variant T/C,G snp 0.22; 3.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs11067228
rs11067228
3 0.923 0.071 12 114656455 intergenic variant A/G snp 0.36 0.010 1.000 1 2013 2013
dbSNP: rs11079344
rs11079344
2 0.923 0.071 17 58297122 intergenic variant A/G snp 0.14 0.010 1.000 1 2012 2012